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Iproclozide is a chemical compound belonging to the class of benzamide fungicides, primarily used for the control of various fungal diseases in crops. It works by inhibiting the demethylation of sterols in the fungal cell membrane, disrupting the synthesis of ergosterol, an essential component for fungal growth and survival. Iproclozide is effective against a wide range of fungal pathogens, including powdery mildew, rust, and leaf spot diseases. It is considered a contact fungicide, meaning it provides protection only where it is directly applied, and has a low risk of resistance development due to its unique mode of action. However, it is important to follow proper application guidelines and resistance management strategies to ensure its continued effectiveness in agricultural practices.

3544-35-2

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3544-35-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3544-35-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,4 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3544-35:
(6*3)+(5*5)+(4*4)+(3*4)+(2*3)+(1*5)=82
82 % 10 = 2
So 3544-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H15ClN2O2/c1-8(2)13-14-11(15)7-16-10-5-3-9(12)4-6-10/h3-6,8,13H,7H2,1-2H3,(H,14,15)

3544-35-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-chlorophenoxy)-N'-propan-2-ylacetohydrazide

1.2 Other means of identification

Product number -
Other names 4-Chlorphenoxy-essigsaeureisopropylhydrazid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3544-35-2 SDS

3544-35-2Downstream Products

3544-35-2Relevant academic research and scientific papers

Decarboxylative hydrazination of unactivated carboxylic acids by cerium photocatalysis

Yatham, Veera Reddy,Bellotti, Peter,K?nig, Burkhard

supporting information, p. 3489 - 3492 (2019/03/26)

We report the cerium photocatalyzed radical decarboxylative hydrazination of carboxylic acids with di-tert-butylazodicarboxylate (DBAD). The operationally simple protocol provides rapid access to synthetically useful hydrazine derivatives and overcomes current scope limitations in the photoredox-catalyzed decarboxylation of carboxylic acids.

Hydrazides as monoamine oxidase inhibitors. Hansch and Free Wilson correlations

Fulcrand,Berge,Noel,et al.

, p. 177 - 182 (2007/10/09)

Some hydrazides of phenoxyacetic acids were synthesized and tested as monoamine oxydase inhibitors. Quantitative structure-activity relationships have been established with the Hansch and Free-Wilson methods. The importance of substitution in the oxidability of the hydrazide group is shown.

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